Support the Pharmacovigilance program with the collection and review of safety data from clinical trials and the set up of related documents in compliance with current regulations. Main Responsibilities Maintain and manage the relation with other Sponsors o oversight and support for all clinical trial pharmacovigilance activities o exchange and migration of safety data o

This position will oversee the global eTMF (electronic Trial Master File) operations for GRD R&D including providing support to all study teams members involved in eTMF management. Responsible for creation and revision of all eTMF associated procedures, ensuring they are up to date and compliant with the applicable regulations. This position will assume the leadership rol